Ulf Pettersson

Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.

W J Kleijer, U. Pettersson, M. Bondeson, 1995, Human molecular genetics.

Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene.

U. Pettersson, N. Dahl, M. Lagerström, 1990, American journal of human genetics.

Molecular and phenotypic variation in patients with severe Hunter syndrome.

R. Gibbs, D. Nelson, S. Dugan-Rocha, 1997, Human molecular genetics.

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1).

U. Landegren, U. Pettersson, Y. Nakahori, 1991, Genomics.